Shenzhen Leaflife Technology Co., Ltd., established in 2015 year, is located in Shenzhen city as the innovation capital of China. It is a high-tech company integrating R & D, manufacturing and marketing of professional medical, beauty and personal beauty equipment, technologies and services. The products are sold to more than 80 countries around the world, with annual sales of more than RMB 80 million.
In 2020, a new 1800m² factory was built in Nantong, Jiangsu, which is specially used for the professional production of personal beauty equipment, and with ISO13485 medical system and ISO9001 quality production system certificate.
Core products Planar LED and Cold Plasma series all are patented technology, MDD, FDA, CE and Anvisa etc. certificates all available.
As an innovation-oriented new technology company, Leaflife has strong technology R&D capabilities. Under the background of the design and manufacturing of professional medical equipment, it brings the originality, leadership, and application of high-quality core components and integrated design of personal equipment technology, to provide authentic, high-tech, high-performance and high-quality product series.
Leaflife is committed to total customer satisfaction by providing consistently high quality products that meet and exceed the expectations of our worldwide customers.
Leaflife quality certified ISO 9001:2008, 13485:2012 systems supports its philosophy and mission to continuosly provide the highest quality.
Leaflife Medical products carry the CE marking according to European directive 93/42.
Leaflife Medical products comply with the specific regulations and standards of the countries in which they are offered for sale.
EC Certificate Directive93/42/EEC on Medical Device – The design, manufacture of laser therapy devices and non-laser light therapy devices for the treatment of hirsutism. Certification by BSI Group.
ISO 13485:2016 & EN ISO 13485:2016 – The design, development, manufacture and distribution of laser therapy devices and non-laser light therapy devices for the treatment of hirsutism. Certification by BSI Group.
FDA Approved – Powered Laser Surgical Instrument, Regulation Number 878.4810, Classification Product Code GEX. 510(K) Number:K202980